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CompletedNCT04108559Updated Dec 26, 2019

Comparison of The Surgical Drain Placement With Use of Kinesiologic Tape

An interventional study of Kinesiologic Tape Group and Drain Group in Impacted Third Molar Tooth, sponsored by Konya Necmettin Erbakan Üniversitesi. Completed at 1 site in Turkey. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-12-26.

Sponsored by Konya Necmettin Erbakan Üniversitesi · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

The investigator's purpose was to compare the effects of the surgical drain and kinesiologic tape applications on postoperative morbidity after mandibular third molar surgery.

Read the detailed description

A total of 90 patients will be scheduled for impacted third molar surgery. The patients will be divided into 3 groups.All surgeries will be carried out by the same surgeon. Group A will be treated with kinesiologic tape, Group B will be treated with a surgical drainage tube and Group C will be control group. After surgery in control group, routine surgical extraction will be performed.The investigators will compare postoperative pain, swelling, trismus and patients' comfort.

The duration of each procedure from the start of the incision to the time of last suture placement will be noted.

Patients are recalled on days 2, 7, 14 postoperative pain, facial swelling, maximum mouth opening, wound dehiscence. For the assesment of the pain, visual analog scale will be used. For the swelling evaluation, measurement will be done from the different three region on the face:

  • Tragus-Pogonion
  • Tragus-Labial Commissura
  • Angulus Mandible-Lateral canthus

Maximum mouth opening will be noted before and after (one week later) the surgery.

02

Conditions studied

  • Impacted Third Molar Tooth

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Keywords

  • Kinesiology tape
  • Surgical drain
  • Pain
  • Swelling
  • Trismus
03

In context

Tooth, Impacted

195 studies on the registry are indexed under Tooth, Impacted; 20 are open to participants now.

This study's enrollment of 30 is below the median of 53 across 164 interventional studies indexed under Tooth, Impacted.

Browse Tooth, Impacted studies →

Lead sponsor

Konya Necmettin Erbakan Üniversitesi is the lead sponsor of 27 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Older than 18 of age,
  • Asymptomatic bilateral mesioangular impacted mandibular third molar (Pell and Gregory class II, position B)
  • Fully covered with mucosa and bone

Exclusion criteria

Exclusion Criteria:

  • Alcohol abuse,
  • Smoking,
  • Pregnancy,
  • No allergy
  • Presence of acute severe periodontitis.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Participant)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Kinesiologic Tape Group

    After the routine impacted third molar surgery, the kinesiologic tape will be prepared individually for each patient; it will be cut into three equal strips (approximately 1.6 cm in width) and placed between the clavicle and the tragus-commissura line. Kinesiologic tape will be removed on the second postoperative day, and all sutures on will be removed on 7. postoperative day.

    Procedure: Kinesiologic Tape Group

  • Experimental
    Surgical Drain Group

    After routine impacted third molar surgery, plastic non-customised drain tube (2-cm long, 2-mm diameter) will be inserted into a vertical incision between the first and second molars and sutured to the vestibular mucosa.

    Procedure: Drain Group

  • Placebo comparator
    Control Group

    Routine third molar extraction will be performed. No extra procedures will be done after surgery.

    Other: Control Group

Interventions

  • ProcedureKinesiologic Tape Group

    A mucoperiosteal flap will be raised, a conventional rotary handpiece will be used under irrigation for removing the third molar.Primary wound closure will be accomplished using 3-0 silk sutures.The kinesiologic tape will be prepared individually for each patient; it will be cut into three equal strips (approximately 1.6 cm in width) and placed between the clavicle and the tragus-commissura line. The patients will be invited after one week for removing the sutures.

  • ProcedureDrain Group

    A mucoperiosteal flap will be raised, a conventional rotary handpiece will be used under irrigation for removing the third molar.Primary wound closure will be accomplished using 3-0 silk sutures. A plastic non-customised drain tube (2-cm long, 2-mm diameter) will be inserted into a vertical incision between the first and second molars and sutured to the vestibular mucosa. The patients will be invited after one week for removing the sutures.

  • OtherControl Group

    Routine third molar extraction will be performed. No extra procedures will be done after surgery.

06

What researchers measure

Primary outcomes

  1. Swelling will be assessed using paper ruler. Tragus-Pogonion Tragus-Labial Commissura Angulus Mandible-Lateral canthus.

    Swelling measurement will be done from the different three region on the face. Tragus-Pogonion Tragus-Labial Commissura Angulus Mandible-Lateral canthus. The swelling measurement will be done preoperatively, postoperative 2nd day, 7th day after the surgery.

    Time frame: Up to 1week

  2. Pain will be assessed using a visual analogue scale.

    The level of postoperative pain will be evaluated using a 10-cm visual analogue scale , with zero representing no pain and 10 representing excruciating pain. Pain measurement will be done everyday in one week after the surgery.

    Time frame: Up to 1week

  3. Trismus will be evaluated using a caliper at maximum mouth opening.

    Trismus will be assessed by measuring the maximum interincisal opening (in millimetres) - the distance between the incisal margin of the upper and lower central incisors. Trismus measurement will be done preoperatively, postoperative 2nd day, 7th day after the surgery.

    Time frame: Up to 1week

07

Study locations

1 site
  • Necmettin Erbakan University
    Konya, Karatay 42050, Turkey
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 26, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04108559
Lead sponsor
Konya Necmettin Erbakan Üniversitesi
Responsible party
Dilek Menziletoglu (Principle Investigator, Konya Necmettin Erbakan Üniversitesi) — Principal investigator
First posted
Sep 30, 2019
Start date
Aug 26, 2019
Primary completion
Dec 18, 2019
Completion
Dec 19, 2019
Last update
Dec 26, 2019

Study contacts

Dilek Menziletoglu, Dr
principal investigator · Necmettin Erbakan University
Bozkurt Ku Isik, Prof Dr
study director · Necmettin Erbakan University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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